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HRID 80162作成日:2026年10月26日

1,2-Diaminocyclohexane, trans- → 1-Benzothiazol-6-yl-3-(6-methyl-pyridin-3-yl)-imidazolidin-2-one

https://huagongshe.com/reaction/80162

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-Diaminocyclohexane, trans-HCID 43806—
反応物Potassium Phosphate, TribasicHCID 62657—
反応物5-Bromo-2-methylpyridineHCID 1201020—
反応物1-Benzothiazol-6-yl-imidazolidin-2-oneHCID 66678554—
触媒Copper iodideHCID 83717—
溶媒1,4-DioxaneHCID 31275—
生成物1-Benzothiazol-6-yl-3-(6-methyl-pyridin-3-yl)-imidazolidin-2-oneHCID 5963622351.8%

反応手順

Using the same reaction conditions as in Example 14, 1-benzothiazol-6-yl-imidazolidin-2-one (I-84b: 150 mg, 0.685 mmol) was reacted with 5-bromo-2-methyl-pyridine (140.5 mg, 0.822 mmol), 1,4-dioxane (10 mL), copper iodide (12.92 mg, 0.068 mmol), trans-1,2-diamino cyclohexane (23 mg, 0.205 mmol) and potassium phosphate (435 mg, 2.055 mmol) to afford the crude product. Purification by column chromatography on silica gel (2% MeOH in CHCl3) afforded 110 mg of the product (51.80% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号USRE045173E1
出典データセットuspto-grants-2014_09
ORD IDord-7f4e3ad1031d4dd98ac262ba4203cc8c
出典メモuspto-grants-2014_09